Thursday 10 Feb 2022
4:00 PM (CET) / 10:00 AM (EST) / 7:00 AM (PST)
approx. 60 min
Dr. Andreas Birk
Founder and Principal Consultant of Software. Process. Management
Medical device development with its regulatory requirements is often viewed unsuited for Agile methods. However, such perceived challenges can be overcome, unlocking Agile’s potential to bring important benefits to the development of medical devices.
This presentation introduces specific Agile practices that are particularly important for medical device development. Examples are: Definition of Done, traceability between agile work items, and building compliance incrementally.
The presentation explains how these practices can be introduced in your development environment, and how they can be supported effectively through state-of-the-art tool infrastructures. The recommendations are substantiated by experience reports from leading healthcare organizations.
What to expect:
- Importance and challenges of Agile in MedTech
- Approaches and best practices for Agile in MedTech
- Solution elements of advanced tool support
The webinar’s agenda:
- Challenges of Agile in MedTech
- Best Practices for Agile in MedTech
- Definition of Done
- Building up Compliance Incrementally
- Requirements Traceability
- Hybrid Development
- Experience & Recommendations
Our webinar is intended for:
Project Managers and Team Leaders, Product Quality and Test Engineers, Heads of Testing & QA teams, Embedded Software Developers, Business Analysts, Regulatory Compliance Analysts
Dr. Andreas Birk is the founder and principal consultant of Software.Process.Management. He helps organizations optimally design and improve their software development processes. His focus areas are software product management, Agile development, and tool-based requirements management.